Tag | Content |
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EnhancerAtlas ID | HS060-07608 |
Organism | Homo sapiens |
Tissue/cell | GM12891 |
Coordinate | chr12:26625840-26626860 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EWSR1-FLI1 | MA0149.1 | chr12:26626525-26626543 | TCTTCCTTGCCTTCTTCC | - | 6.44 | RARA | MA0729.1 | chr12:26626502-26626520 | CCTTGCCTTTTTGACCTT | - | 6.34 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr12 | 26626326 | 26626794 | chr12 | 26626200 | 26626800 |
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| Number: 1 | ID | Chromosome | Start | End |
GH12I026473 | chr12 | 26625934 | 26626930 |
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Enhancer Sequence | ACAGAGTCTT GCTCTATCGC CCAGGATGGA GTGCAGTGGA GTGATCTAGG CTCACTGCAA 60 CCTCCACCTT CCAGGTTCAA GTGATTCTCG TGCCTCAGCC TCCTAAGCAG CTTGGATTAC 120 AGTCATGCAC CACCACACCC AACTAATTTT TGTATTTTTA GTACAGATGA GGTTTCACCA 180 TGTTAGCCAG GCTGCTCTTG AACTCCTGAC TTCAAGTGAT CCACCCACCT CAGCCTCCCA 240 AAGTCTTGGG ATTACAGGCG TGAGCCATTG CACCTGGCCT GTATCCTCTA CTTTTATGCT 300 TAGTCTGCTT CAAACTGAAG TTACCTAACA TAAGTCTTTT CTTTACCTTG ATATTTTCAC 360 TGTTACCCCT AAGACACTGG TCATCTGAGA CTGCTTTATT AAATTTCTTA ATGGATGTCA 420 GGTGGTTCAT TCATTGTCTG CTGGCCAATC TGTCACTCTG CTGGCTCCAG GGCAAGCTTA 480 GCTCATCTGG TTGTTCATTC CCCACTCAAC AGCTACACAG TCAGGTTTTA CTCATGCAGC 540 TGCTCACTCG TGCAAGAAGA CAACCTCCCC CATACAAAGC AAGACTATCT TGCAGTCAAG 600 AAAACAGAAG TGGTTCTACT TCCCTACTTT CTTCTTCTGA AACTTATTAC TGCTCATTTT 660 GACCTTGCCT TTTTGACCTT GCTTGTCTTC CTTGCCTTCT TCCCTCCACA GTGCTACAGC 720 CTCTAAAGTA ACTCCTTGAC CCTGTACACA TATGGGTCAG CATGTTTCTG TGTTCATTCT 780 AGTAGCCAAT ATGATTTTAA TTCTCAGCCT GGGATTTTTT CCTTTCTACT CACATTCAAT 840 CTCTAGCCAT TCCTTTGCTA GCTTGACTCA CTTTGTGTCA CATGGCTTCT CTTTCTCTCT 900 AAAACGACAC CTTTTCCACA TCCTAAATCT CCACTTTCTG CTTCCTTCCA CTTGTCCATC 960 ATCCTGGCTT TCAGTTGCTC AGCAGCTAAA ATGCTCATCT GTCTAGCTAT AAGTCATCTG 1020
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